4-(3-(4-phenyl-piperidino)-2-hydroxy-propoxy)-benzophenones

ABSTRACT

NOVEL LOWER ALKYLOXY BENZOPHENONE DERIVATIVES AND PROCESSES FOR THEIR PREPARATION ARE DISCLOSED. THESE NOVEL BENZOPHENONE DERIVATIVES ARE USEFUL AS PSYCHOSEDATIVE AGENTS.

3,816,434 4-[3-(4 PHENYL PIPERIDINO) 2 HYDROXY- PROPOXY]-BENZOPHENONES Albrecht Edenhofer, Riehen, Henri Ramuz, Birsfelden, and Hans Spiegelberg, Basel, Switzerland, assiguors to Holfmann-La Roche Inc., Nutley, NJ.

No Drawing. Application May 21, 1970, Ser. No. 39,505, now Patent No. 3,706,755, dated Dec. 19, 1972, which is a continuation-impart of application Ser. No. 567,354, July 25, 1966, now abandoned. Divided and this application Apr. 19, 1972, Ser. No. 245,609

Int. Cl. C07d 29/20 U.S. Cl. 260-293.8 2 Claims ABSTRACT OF THE DISCLOSURE Novel lower alkyloxy benzophenone derivatives and processes for their preparation are disclosed. These novel benzophenone derivatives are useful as psychosedative agents.

This application is a divisional application of Ser. No. 39,505, filed May 21, 1970, and now U.S. Pat. 3,706,755, issued Dec. 19, 1972, which in turn is a continuation-inpart of Ser. No. 567,354, filed July 25, 1966 and now abandoned.

DESCRIPTION OF THE INVENTION R is selected from the group consisting of wherein the character n represents from -2 double bonds; R is hydrogen or hydroxy; R is hydrogen, lower alkyl, lower alkoxy, or halogen; R and R are each selected from the group consisting of hydrogen, lower alkyl, lower alkoxy, halogen, cyano, carboxy, nitro, amino and trifluoromethyl; Y is selected from the group consisting of carbonyl, methylene, hydroxymethylene and hydroxyiminomethylene; and X is selected from the group consisting of carbonyl, hydroxymethylene, acyloxymethylene, alkoxycarbonyloxymethylene and dihydroxyphosphinylmethylene the pharmaceutically acceptable acid addition salts thereof, the quaternary salts thereof with quaternizing agents, the ketals thereof and optical isomers thereof.

United States Patent 0 Representative of the compounds of formula I above are:

4- [3,6-Dihydro-4-phenyl-1 (2H) pyridyl) -2-hydroxypropoxy]-benzophenone 4- 3- (3,6-Dihydro-4-phenyl-l 2H) pyridyl) -2-hydroxypropoxy]-4-chlorobenzophenone 4- 3- (4- (p-Chlorophenyl) -3,6-dihydro-l (2H) pyridyl) 2-hydroxy-propoxy]-benzophenone 4- 3- (4- p-Chlorophenyl) -3,6-dihydro-1 2H) pyridyl)- 2-hydroxy-propoxy]-4'-chlorobenzophenone 4- [3- 3,6-Dihydro-4-phenyl-1 (2H pyridyl) -2-hydroxypropoxy] -4-fluorobenzophenone 4- 3-(4- (p-Fluorophenyl)-3,6-dihydro-l 2H) pyridyl) 2-hydroxy-propoxy]-4-fluorobenzophenone 4- 3- (4- (p-Fluorophenyl)-3,6-dihydro-l 2H) pyridyl) 2-hydroxy-propoxy] -4'-chlorobenzophenone 4-[3-(4-(p-Chlorophenyl)-3,'6-dihydro 1(2H)pyridyl)-2- hydroxy-propoxy] -4-fluorob enzophenone 4-[3(4-(p-Fluorophenyl)-3,6-dihydro 1(2H)pyridyl 2- hydroxy-propoxy]-4'-bromobenzophenone v 4-[3-(4-(p-Chlorophenyl)-3, 6-dihydro l(2H)pyridyl)-2- hydroxy-propoxyl-4'-bromobenzophenone 4-[3-(4-(p-Chlorophenyl) 1 piperazinyl) 2 hydroxypropoxy]-benzophenone 4-[3-(4-(p-Chloropheny1) l piperazinyl) 2 hydroxypropoxy] -4'-fluorob enzophenone.

A preferred group of compounds falling within the scope of Formula I are those wherein R is hydrogen or halogen and R is hydrogen, i.e. a compound of the formula CHzXCHz-R R1 wherein R is hydrogen or halogen and X, Y and R are as described above.

Another preferred group of compounds falling within the scope of Formula I are those wherein Y signifies a carbonyl group, i.e. compounds of the formula wherein R, R R and X are as described above.

A further preferred embodiment of the present invention are those compounds falling within the scope of Formula I wherein X signifies hydroxymethyl and Y signifies a carbonyl group, i.e. compounds of the formula OCH: CH-CHz-R R1 5 where R, is as described above.

3 Preferred are those compounds of the Formula I wherein X is hydroxymethylene and Y is carbonyl. Especially preferred are compounds as in the last sentence wherein R is hydrogen or halogen, R and R are both hydrogen, and R is hydrogen, halogen or lower alkoxy,

i.e. compounds of the formula is -es H0 wherein R is selected from the group consisting of hydrogen and halogen; R is hydrogen, halogen or lower alkoxy; and the dotted lines indicate the option of having none, one or two double bonds.

Most preferred of the compounds of Formula I are:

4- [3 (3,6-Dihydro-4-phenyl-1 (2H -pyridyl) -2-hydroxyprop oxy] -benzophenone 4- 3-(4- (p-Fluorophenyl -3,6-dihydro-l 2H) -pyridyl)- Z-hydroxypropoxy] -4'-chloro-benzophenone 4- [3- (4- (p-Fluorophenyl) -3,6-dihydro-l (2H)-pyridyl) 2-hydroxypropoxy) -4'-fluoro-b enzophenone 4- [3- (4- (p-Chlorophenyl) -3,6-dihydro-1 (2H) -Pyridyl)- Z-hydroxypropoxy] -4-chloro-benzophenone 4- [3- (4- (p-Methoxyphenyl) -1-piperazinyl)-2-hydroxypropoxy] -4'-fluoro-benzophenone 4- 3- (4-( p-Methoxyphenyl l-piperazinyl) -2-hydroxypropoxy] -4-chloro-benzophenone.

The term lower alkyl as utilized throughout the present disclosure is intended to designate straight or branched chain hydrocarbon groups having from 1-7 carbon atoms, most preferably, from 1-5 carbon atoms in the chain. Representative of such are methyl, ethyl, propyl, isopropyl, butyl and the like. The term halogen is intended to connote all 4 forms thereof, e.g. fluorine, chlorine, bromine and iodine unless otherwise specified. Especially preferred among the members of the halogen family for the purposes of the present invention are fluorine, chlorine and bromine, most advantageously, fluorine and chlorine. The term lower alkoxy as employed herein connotes a straight or branched hydrocarbonoxy chain containing 1-7 carbon atoms, preferably 1-5 carbon atoms, such as methoxy, ethoxy, isopropyloxy and the like. By the term acyl there is intended groupings bearing a terminal C=O grouping joined to a carbon atom, such as benzoyl and an acyl moiety of a lower alkanoic-acid, e.g. acetyl, propionyl and the like.

As is evident from the above, when n is 0, i.e. wherein the heterocyclic moiety in the group designated by the character R contains no double bonds, i.e., is saturated, then piperidino or piperazinyl is intended. Similarly, if n is 1 or 2, i.e., the heterocyclic moiety contains one or two double bonds, there is represented dihydropyridinyl, tetrahydropyridinyl, dihydropyrazinyl, tetrahydropyrazinyl and substituted derivatives thereof. The introduction of the heterocyclic moiety may be effected by the utilization of an appropriate starting material containing the corresponding heterocyclic moiety. Alternatively, an unsaturated heterocyclic moiety, i.e. wherein n in the Formula I is 1 or 2, can be provided in the end product of Formula I above by the use of an appropriate starting material containing an unsaturated heterocyclic moiety and the so-formed compound containing such an unsaturated heterocyclic moiety can be reduced by hydrogenation in a manner more fully described hereinafter.

The novel compounds of the Formula I can be prepared using a wide variety of reaction routes. In one such preparative technique, a compound of the Formula I above is obtained by reacting a corresponding compound of the formula oomz R; A I i B wherein R R and Y are as described above and Z is selected from the group consisting of X'-CH --R and where X represents a member selected from the group consisting of carbonyl or hydroxymethylene and R is halogen, preferably chlorine or bromine, alkyl sulfonyloxy, preferably mesyloxy and aryl sulfonyloxy, preferably tosyloxy; and ketals or diketals thereof with a compound of the formula (III) wherein R is as described above.

In another reaction route leading to the compounds of Formula I above, a compound of the formula OH R wherein R and R are as above and Y' is selected from the group consisting of carbonyl, methylene and hydroxymethylene; or a ketal of this compound is reacted with a compound of the formula wherein R is described above and M is selected from the group consisting of R is as described above, i.e. compounds of the formula wherein R and R are as described above may be prepared by reacting a compound of the formula wherein R and R are as described above with a compound of the formula wherein R is as described above.

In a further process aspect of the present invention, compounds of Formula If above may be prepared by reacting a compound of the formula (VII) wherein R and R are as described above.

In another process aspect, compounds of Formula If above wherein R is lower alkoxy may be prepared by introducing a lower alkoxy group by conventional means into a compound of the formula 0 omoHorn-N' N Q 0H I OH 0 wherein R is as described above.

Compounds of the Formula I above wherein X or Y is carbonyl (or the intermediates utilized in the process of preparing same which contain a carbonyl group) can be converted into a ketal by treating the same with an alcohol such as a lower alkanol, e.g. methanol or a polyhydroxyalcohol such as ethylene glycol, in the presence of, for example, calcium chloride or a trace of acid according to techniques well established in the art. The term ketal is often used interchangeably by those skilled in the art with the term aceta The product of the Formula I above, if it contains an unsaturated heterocyclic moiety, can be hydrogenated or if it contains a carbonyl group, can be ketalized or diketalized or reduced or converted to an oxime by reaction of a compound of Formula I, wherein Y is carbonyl with hydroxylamine hydrochloride. A compound containing a hydroxymethylene group can be oxidized or esterified by conventional procedures for effecting esterification. Furthermore, the products obtained from the preparative techniques described above can be converted into a quaternary ammonium compounds with a quaternizing agent or into the acid addition salt thereof with pharmaceutically acceptable acids and/or split into the corresponding optical isomers.

Compounds of the Formula I above wherein the group R includes an unsaturated heterocyclic moiety, i.e. wherein in the Formula I above, It is 1 or 2, can be hydrogenated to obtain the saturated derivatives thereof. For example, the compounds of the Formula I which contain such unsaturated heterocyclic moieties can be converted into the corresponding compounds which contain a saturated heterocyclic moiety by hydrogenating the former conventionally in the presence of a noble metal catalyst system such as palladium/charcoal, preferably, in a solvent medium such as methyl or ethyl alcohol whereby to obtain the desired compounds, i.e. one in which the group R in Formula I above includes the piperidinyl or piperazinyl moiety.

As is evident from the above, the groups represented by the characters Y, Y, X and X" can be converted one unto the other, if desired, by various procedures. For example, a compound of the Formula I above wherein X connotes a carbonyl group and Y a carbonyl or a methylene group, can be obtained by oxidizing the corresponding compound wherein X or X is hydroxy methylene and Y or Y is a carbonyl or a methylene group with a mixture of dimethylsulfoxide and acetic acid anhydride.

If Y or Y connotes the carbonyl group, compounds of the Formula I above wherein Y connotes a hydroxyirninomethylene group can be obtained via the reaction with hydroxylamine. Should X or X be a carbonyl group, it would be necessary to first ketalize same in order to protect this carbonyl group from reacting with the hydroxyl amine. The protecting ketal group, if desired, can be removed by hydrolysis after formation of the hydroxyiminomethylene group according to techniques well established in the art.

Reduction of a carbonyl group Y into the hydroxymethylene or methylene group can be carried out in the same manner as for the starting compounds of Formula II below.

Compounds of the Formula I above can be converted into the corresponding quaternary ammonium compounds by treating same with a quaternizing agent such as an alkali halide, e.g. methyl iodide. The treatment is advantageously effected utilizing an excess of the quaternizing agent in the absence of a solvent.

Compounds of Formula 1 above, form pharmaceutically acceptable acid addition salts with inorganic and organic acids, such as hydrohalic acids, e.g. hydrochloric acid and hydroiodic acid, with other mineral acids such as sulfuric acid, phosphoric acid, nitric acid or with organic acids such as tartaric acid, citric acid, oxalic acid, camphor sulfonic acid, ethane sulfonic acid, toluene sulfonic acid, mandelic acid, salicylic acid, ascorbic acid, maleic acid and the like. Among the many acid addition salts suitable for the purposes of the present invention, especially preferred is the hydrohalic acids, most preferentially, hydrochloric acid. The acid addition salts are advantageously prepared in a suitable solvent such as ethanol by treating the free base with the corresponding nonaqueous acid.

Compounds of the Formula II above which are useful as starting materials in the preparation of the compounds of the Formula I above can be prepared as follows:

A compound of the Formula H in which X' designates a hydroxymethylene group and Y a carbonyl group can be prepared via the reaction of a 4-alkoxybenzoyl halide with benzene or a substituted derivative thereof in the presence of an aprotic Lewis acid, such as for example, aluminum chloride, zinc chloride, boron trifluoride and the like (by Friedel-Crafts techniques). The so-formed compound is dealkylated to prepare a 4-hydroxy-benzophenone which is in turn reacted with an excess of an epihalohydrin, especially epichlorohydrin to thus prepare a corresponding compound of the Formula II above wherein X designates a hydroxymethylene group, Y a carbonyl group and Z a grouping. The reaction with an excess of an epihalohydrin is effected in the presence of a catalytic amount of any suitable organic base such as piperidine, at elevated temperatures, most preferably at about C.

Also, the 4-hydroxy benzophenones, i.e. compounds of the Formula IV above wherein Y is carbonyl, can additionally be prepared via the reaction of a 4-alkoxy benzoic acid with benzene, either substituted or unsubstituted, by condensing the two in the presence of polyphosphoric acid and dealkylating the compound so prepared.

4-hydroxy benzophenones in an advantageous process aspect of the present invention, can be prepared from the corresponding phenyl benzoate by Fries rearrangement in a manner well known in the art.

Compounds of the Formula II above in which X and Y designate a hydroxymethylene group can be prepared by reducing selectively the correspondingly substituted 4- hydroxy benzophenone and joining same to the appropriately constituted side chain. Alternatively, a compound of the Formula II above wherein Y and X' are carbonyl can be reduced to effect the same end. The reduction in either case is effected with a metal hydride, for example, with a lower alkali metal borohydride, e.g. sodium borohydride or with an alkali metal aluminum hydride such as lithium aluminum hydride. Alternative compounds of the Formula II above in which X and Y represent a hydroxymethylene group can be prepared by reacting the corresponding substituted benzaldehyde with a p-alkoxybenzene magnesium bromide (a Grignard reagent), to yield after dealkylation, the corresponding 4-hydroxy-benzhydrol and joining the appropriate side-chain thereto.

Compounds of the Formula II in which X' connotes a hydroxy methylene group and Y designates a methylene group can be prepared by reacting the corresponding hydroxybenzophenone of the Formula IV above according ot the WolflF-Kishner technique, i.e. after conversion to a semicarbazone or hydrazone, e.g. in the presence of an alkali alcoholate such as sodium methoxide at elevated temperatures. The same end can be eflfected via a Clemmensen rearrangement. For example, reducing in the pres ence of a catalyst, e.g. amalgamated zinc and hydrochloric acid, and thereafter, treating the so-obtained reduced product with epihalohydrin, preferably epichlorohydrin.

Compounds of the Formula II in which X represents an hydroxymethylene group and Y a hydroxyiminomethylene group can be prepared by treating the corresponding compound of the Formula II above wherein Y is carbonyl with hydroxylamine hydrochloride.

Compounds of the Formula II wherein X connotes a hydroxy methylene group and Y connotes a carbonyl group can be oxidized to compounds of the Formula II above wherein X and Y are both carbonyl groups with conventional oxidizing agents, e.g. with potassium per- -manganate or sodium dichromate.

By oxidizing compounds of the Formula II above wherein X' represents a hydroxy methylene group and Y represents a methylene group, there can be obtained a compound of the Formula II in which X connotes a carbonyl group and Y connotes a methylene group. The oxidation can be effected by any suitable oxidation system capable of effecting this end. Preferred for this purpose is a mixture of dimethylsulfoxide and acetic acid anhydride.

Compounds of the Formula II wherein R represents halogen or alkyl sulfonyloxy (e.g. mesyloxy) or an aryl sulfonyloxy (e.g. tosyloxy) can be converted into compounds of the Formula II which contains the grouping (mic...)

according to techniques well established in the art such as those described below in connection with compounds of the Formula V.

Compounds of the Formula III can be prepared in accordance with conventional procedures.

The reaction of a compound of the Formula H with a compound of the Formula III proceeds efi'icaciously at a temperature of from about room temperature to about the boiling point of the reaction medium. Most preferred is a temperature range of from about 70 to about 100 C. Suitably, the reaction is run in the presence of an inert organic solvent medium, for example, in dimethylsulfoxide, an alkanol such as methanol, ethanol, isopropanol and the like or a cyclic ether such as tetrahydrofuran and dioxane and the like.

Compounds of the Formula II in which R represents halogen or alkylsulfonyloxy or arylsulfonyloxy (especially, respectively, mesyloxy or tosyloxy) is preferentially reacted with a compound of the Formula III in the presence of an acid acceptor. Among the many acid acceptors suitable for this purpose can be included pyridine and the like. A compound of the Formula II above in which Z connotes the group (aria...)

can be directly reacted with a compound of the Formula III above without the necessity of an acid acceptor being present to thereby obtain the corresponding compound of the Formula I above.

Techniques for preparing compounds of the Formula IV above are described hereinabove.

Compounds of the Formula V in which X connotes a hydroxy-methylene group, can be prepared, for example, via the reaction of the base of the Formula III above with an epihalohydrin, most preferentially, with epichlorohydrin, in the presence of an aqueous alkanol such as ethanol at elevated temperatures whereby to prepare a compound of the Formula V in which R, is halogen. The resulting product, by treatment with strong aqueous alkali at room temperature, can be converted into compounds of the Formula V wherein M is Compounds of the Formula V above in which R connotes an alkylsulfonyloxy group or an aryl sulfonyloxy group, particularly, mesyloxy and tosyloxy, respectively, are similarly capable of being converted into a compound of the Formula V above wherein M is a O -C- CH: grouping.

Compounds of the Formula V above in which X designates a carbonyl group can be prepared from the corresponding compound of the Formula V above wherein X" designates hydroxymethylene, by oxidizing the lastmentioned compound with a mixture of dimethyl sulfoxide and acetic anhydride whereby to convert the hydroxymethylene group into the desired carbonyl group. While temperature and pressure are not critical aspects of this process step, it is preferred to perform the oxidation at room temperature.

Compounds of the Formula V can be reacted with a compound of the Formula IV under the same reaction conditions as described above in connection with the reaction of a compound of the Formula II with a compound of the Formula III. If M in the Formula V above includes the grouping R CH X", the compound of the Formula IV is preferably first converted to an alkali metal salt, for example a sodium or potassium salt (e.g. by treatment with an alkali metal hydroxide, such as sodium or potassium hydroxide or an alkali metal alcoholate such as sodium or potassium methylate) prior to the reaction with a compound of Formula V or the reaction of the compound of Formula IV with a compound of Formula V is carried out in the presence of a tertiary organic base, preferably, pyridine, a tri-lower alkyl amine such as triethylamine and the like.

The starting materials of Formula VI are obtained in a suitable manner by reaction of the respective 4-(2,3- epoxypropoxy)-4'-halobenzophenone with ethylenimine and subsequent reaction of the 4-(3-aziridinyl-2-hydroxypropoxy)-4'-halobenzophenone obtained with p-anisidine. Both reaction steps are preferably conducted in the presence of a lower alkanol (e.g. methanol) at a temperature between approximately 0 C. and 50 C. The last reaction step is carried out preferably in the presence of an acid such as, for example, maleic acid, a hydrohalic acid (e.g. hydrochloric acid), hydrotrifluoroboric acid or a borotrifluorideacetic acid complex.

The starting material of Formula VI can be obtained also by reaction of the respective 4-(2,3-epoxypropoxy)- 4'-halobenzophenone with N-(2-aminoethyl)-p-methoxyaniline.

The reaction of the compounds of Formulas VI and VII is efiicaciously performed in the presence of a polar organic solvent, such as a lower alkanol (e.g. methanol, ethanol) or in dimethylformamide, dimethylsulfoxide or tetrahydrofuran. A suitable reaction temperature is between approximately 50 C. and the boiling point of the reaction mixture. The reaction is performed in the presence of an acid-binding substance, e.g. in the presence of an alkali metal carbonate or hydroxide, for example potassium carbonate, sodium hydroxide and the like. 1,2- dichloro-1,2-dibromo or 1,2-ditosyloxy ethane are used as starting materials of Formula VII in preferred methods.

The starting materials of Formula VIII are prepared suitably from the respective 4-(2,3-epoxypropoxy)-4- halobenzophenones. The latter can be rearranged into the respective N-{3- [p-(p'-halobenzoyl)phenoxy]-2-hydroxypropyl}succinimides by reaction with succinimide, preferably in the presence of a lower alkanol (e.g. ethanol); the resulting compounds are converted to the 4-(3-amino- 2-hydroxypropoxy)-4'-halobenzophenones of Formula VIII by subsequent hydrolysis. Acids (e.g. hydrochloric acid) as well as bases (e.g. soda lye) can be used for the hydrolysis.

The subsequent reaction of the compounds of formulas VIII and IX is preferably performed in the presence of a polar organic solvent, such as a lower alkanol (e.g. methanol, ethanol), or also in dimethylformamide, dimethylsulfoxide or tetrahydrofuran. The temperature is suitably between approximately 50 C. and the boiling point of the reaction mixture. The reaction is eflicaciously performed in the presence of an acid-binding substance, e.g. in the presence of an alkali metal carbonate or hydroxide, for example in the presence of potassium carbonate or sodium hydroxide. p-[bis-(Z-chloroethyD- amino]-anisol, p-[bis-(2-bromoethyl)-amino]anisol or p- [bis-(2-tosyloxyethyl)-amino]anisol are preferred as starting materials for Formula IX.

The starting materials for Formula X can be obtained e.g. by the reaction of 1-[p-hydroxyphenyl]piperazine with the respective 4-(2,3-epoxypropoxy)-4'-halobenzophenones. The reaction is carried out to advantage in the presence of a polar organic solvent, e.g. in the presence of a lower alkanol (e.g. ethanol) or in a cyclic ether such as dioxane.

The so-obtained starting materials of Formula X are then methylated. The methylation is performed following conventional techniques, e.g. by converting a compound of Formula X to an alkali metal salt, e.g. the sodium or potassium salt, and subsequent reaction with an alkylating agent such as dimethyl sulfate in an aqueous alkali solution. In an alternate method, the compound of Formula X is mixed with an alkali alkanolate solution, for example in a sodium methylate or potassium methylate solution, and the mixture is reacted subsequently with dimethyl sulfate or a compound of the formula CH T (XI) wherein T is halogen, alkylsulfonyloxy or arylsulfonyloxy in the presence of an alkali metal hydride, preferably sodium hydride. Methyl bromide or methyl iodide are preferred as methylating substances. In a third method, a compound of Formula X is methylated with diazomethane. In this case, the compound of Formula X is dissolved preferably in a lower alkanol, (e.g. methanol, ethanol) and the diazomethane is preferably dissolved in ether solution.

The methylation described above is performed at a low temperature. Temperatures between C. and 40 C. are preferred.

The compounds of the Formula I, as is evident from the structural configuration thereof, occur in two optical isomeric forms. These can be separated according to conventional procedures. For example, the racemate can be resolved by treating the base with an optically active acid, e.g. with tartaric acid, bromo-camphorsulfonic acid and the like. The resulting salts are separated through fractional crystallization into two fractions and the so-obtained fractions are split into their optical antipodes.

Thus, for example, the (+)-form of a compound of Formula If is obtained if, according to the invention, an optical (+)-antipode of a star-ting material of Formula II, V, VI, VII I or X is used. The obtained compound must be racemized. The racemization can be performed, after preceding protection of the keto group (by treating with N,N-dimethylhydrazine and subsequent quaternization of the 'N,N-dimethylhydrazone group with methyl iodide), by the oxidation of the hydroxy group of the side chain to the 0x0 group by means of dimethylsulfoxide and acetic anhydride and subsequent reduction of the obtained oxo group by means of an alkali metal borohydride followed by the cleavage of the quaternary N,N,N-trimethylhydrazone group with mild lye. Another method consists of the exchange of the hydroxy group of the side chain with chlorine with the use of thionyl chloride in chloroform. After treating with alkanolic sodium hydroxide solution, the introduced chlorine atom is again exchanged for a hydroxy group, and a product is formed that contains the (-)-antipode of a compound of Formula If.

If the reacemate is obtained, separation can be carried out, for example, by the rearrangement of the base with an optically active acid, e.g. or )-tartaric acid or a derivative thereof, e.g. or -)-O,O4libenzoyltartaric acid, or ()-a-bromocamphorsulfonic acid, etc. The mixture of the 2 optic isomers can be separated by repeated fractionated crystallization, and the (-)-antipode of a compound of Formula If desired, because of its high level of activity, is isolated.

The bases of Formula I are crystalline, solid substances, soluble in dimethylsulfoxide, dimethylformamide and in chlorinated hydrocarbons, such as chloroform and methylene chloride and relatively insoluble in water, methanol, ethanol, benzene and petroleum ether.

The acid addition salts of the bases of Formula I are also crystalline, solid substances. They are soluble in dimethylsulfoxide and dimethylformamide and relatively insoluble in water, methanol, ethanol, benzene, petroleum ether and in chlorinated hydrocarbons such as chloroform and methylene chloride.

The compounds of the Formula I above, their ketals, quaternary ammonium compounds and acid addition salts are useful in view of their activity on the nervous system. Thus, they are useful as psycho-sedative agents, particularly in view of their capability of acting as reserpine-like hypotensive and sedative agents.

The narcosis potentiating activity of the compounds of Formula I on mice serves to demonstrate their psychosedative activity in warm blooded animals: Ethanol in a concentration of about 4 g./ kg. body weight, injected intraperitoneally, results in an average duration of sleep (side posture) of less than one minute. In mice which have previously been treated with a psycho-sedative preparation, the duration of sleep is prolonged. The prolongation of the duration of sleep serves as a criterion for the psychosedative effect.

A compound of Formula I, as the test compound, was applied per os in the doses set out hereinafter to groups of 10 to 60 mice each (male animals, average weight 18-20 g.). After 15 minutes, ethanol in a dosage of 4 g./-kg. body weight was administered intraperitoneally to all animals as well as to a control group of animals.

Results obtained utilizing the compounds of Formula I as the test compounds in the foregoing procedure are set forth hereinbelow in Table I TABLE I Compound Duration of sleep, p.o. minutes O-GHz-CHOH-CHr-N enema- Mun- The compounds of the Formula I, the acid addition salts thereof and the ketals can be administered in pharmaceutical dosage forms with the dosage adjusted to fit the exigencies of the therapeutic situation. The pharmaceutical dosage form may be prepared by incorporating the active ingredient in solid or liquid vehicles to provide dragees, capsules, elixirs, emulsions, powders and the like according to pharmaceutical practices. The carrier for the dosage form may be, for example, water, gelatin, gum arabic,

polyalkylene glycols, Vaseline and the like. The so obtained dosage forms may be sterilized and/ or may contain additives such as preserving, stabilizing, wetting and emulsifying agents. Other pharmaceutical adjuvants may be incorporated if necessary, such as salts for varying the osmotic pressure.

Convenient pharmaceutical dosage forms contain about 5 to 100 mg. of the compound of Formula I. Convenient oral dosages are in the range of about 0.1 mg. per kg. per

lactose, starch, magnesium stearate, talc, vegetable oils, 75 day to about 10 mg./kg. per day. However, the aforementioned ranges are exemplary only and can be varied upwards or downwards depending upon the requirements of the warm blooded animal being treated and the directions of the physiican.

The following examples are illustrative but not limitative of the present invention. All temperatures are stated in degrees centigrade.

Example 1 12.7 of 4-[2,3-epoxy-propoxy]-benzophenone are dissolved in 50 ml. of dioxan and, after the addition of 8.0 g. of 4-phenyl-1,2,3,6-tetrahydropyridine, heated under reflux conditions for hours. The solvent is subsequently evaporated off under reduced pressure. The residual 4-[3- (3,6-dihydro-4-phenyl-1(2H)-pyridyl)-2 hydroxy propoxyj-benzophenone is dissolved in 20 ml. of ethanol and made congo-acid with ethanolic hydrochloric acid. The hydrochloride which precipitates crystalline melts at 192- 194 alter recrystallization from ethanol.

In an analogous manner, there are obtained when employing:

4 [2,3-epoxy-propoxy]-4'-methoxy-benzophenone and 4-phenyl-1,2,3,6-tetrahydro-pyridine; the compound 4-[3- (3,6-dihydro-4-phenyl-1(2H)pyridyl) 2 hydroxy propoxyl 4 methoxy benzophenone hydrochloride, M.P. 185-186.

4-[2,3-epoxy-propoxy]-3-methyl-benzophenone and 4- phenyl-1,2,3,6-tetrahydro-pyridine; the compound 4 [3-( 3, 6-dihydro-4-phenyl-1(2H)pyridyl)-2-hydroxy propoxy]- 3-methyl-benzophenone, M.P. 200-203".

4-(2,3-epoxy-propoxy)-4-methy1-benzophenone and 4- phenyl-1,2,3,6-tetrahydropyridine; the compound 4-[3-(3, 6-dihydro-4-phenyl-1(2H)pyridyl)-2-hydroxy propoxy]- 4'-methyl-benzophenone hydrochloride, M.P. 209-210".

4-[2,3-epoxy-propoxy] benzophenone and 4-p-fiuorophenyl-1,2,3,6-tetrahydropyridine; the compound 4-[3-(4- p-fluoro-phenyl)-3,6-dihydro-1(2H)pyridyl) 2 hydroxypropoxy]-benzophenone hydrochloride, M.P. 160".

4-(2,3-epoxy-propoxy)-4'-chlorobenzophenone and 4-pchloro-phenyl-1,2,3,6-tetrahydropyridine; the compound 4- [3 (4 (p-chlorophenyl)-3,6-dihydro-1(2H)pyridyl)-2- hydroxypropoxy]-4' chlorobenzophenone hydrochloride, M.P. 212.

4-(2,3-epoxy-propoxy) 4 nitrobenzophenone and 4- phenyl-l,2,4,6-tetrahydropyridine; the compound 4-[3-(3, 6-dihydro-4-phenyl-1(2H)-pyridyl)-2-hydroxy propoxy1- 4'-nitro-benzophenone hydrochloride, M.P. 20l-203.

4-(2,3-epoxy-propoxy)-4'-bromobenzophenone and 4- phenyl-1,2,3,6-tetrahydro-pyridine; the compound 4-[3-(3, 6-dihydro-4-phenyl-1(2H)-pyridyl)-2-hydroxy propoxy]- 4-bromobenzophenone hydrochloride, M.P. 210212.

4-(2,3-epoxy-propoxy)-4'-fluorobenzophenone and 4- phenyl-1,2,3,6-tetrahydropyridine; the compound 4-[3-(3, 6-dihydro-4-phenyl-l(2H)pyridyl)-2-hydroxy propoxy]- 4'-fluoro-benzophenone hydrochloride, M.P. 198-200.

4-(2,3-epoxy-propoxy)-4'-fluorobenzophenone and 4-1:- fiuoro-phenyl-1,2,3,6-tetrahydropyridine; the compound 4- [3-(4- (p-fluorophenyl)-3,6-dihydro-1 (2H)pyridyl)-2 hydroxy-propoxy] 4' fluorobenzophenone hydrochloride, M.P. 192193.

4-(2,3-epoxy-propoxy)-4'-chlorobenzophenone and 4-pfluoro-phenyl-l,2,3,6-tetrahydropyridine; the compound 4- [3-(4-(p-fluoro-phenyl)-3,6-dihydro 1(2H)pyridyl) 2- hydroxy-propoxy]-4'-chlorobenzophenone hydrochloride, M.P. 203204.

4-[2,3-epoxy-propoxy]-4' chlorobenzophenone and 4- phenyl-l,2,3,6-tetrahydro-pyridine; the compound 4-[3-(3, 6-dihydro-4-pheuyl-1(2H)-pyridyl)-2-hydroxy propoxy1- 4-chlorobenzophenone hydrochloride, M.P. 202.

4-[2,3-epoxy-propoxy]-benzophenone and 4-p-chlorophenyl-l,2,3,6-tetrahydro-pyridine; the compound 4-[3-(4- (p-chlorophenyl)-3,6-dihydro-1(2H)pyridyl)-2 hydroxypropoxy]-benzophenone hydrochloride, M.P. 217-218.

4-(2,3-epoxy-propoxy)-4-trifluoromethyl-benzophenone and 4-phenyl-1,2,3,6-tetrahydro-pyridine; the compound 4- 14 [3-(3,6-dihydro-4-phenyl-1(2H)-pyridyl) 2 hydroxypropoxy]-4'-trifluoromethyl-benzophenone hydrochloride, M.P. 231.

4-(2,3-epoxy-propoxy)-3'-chlorobenzophenone and 4- phenyl-1,2,3,G-tetrahydro-pyridine; the compound 4-[3- (3,6-dihydro-4-phenyl-1(2H)pyridyl) 2 hydroxy-propoxy]-3-chlorobenzophenone hydrochloride, M.P. 175

4-(2,3-epoxy-propoxy)-benzophenone and 4 phenyl-4- hydroxy-piperidine; the compound 4-[3-(4-hydroxy-4- phenyl-piperidino) 2 hydroxy-propoxy]-benzophenone hydrochloride, M.P. 184.

4 (2,3 epoxy-propoxy)-3'-trifluoromethyl-benzophenone and 4-p-chloropheny1-1,2,3,6-tetrahydropyridine; the compound 4 [3-(3,6-dihydro-4-phenyl-1(2H)pyridyl)-2- hydroxypropoxy]-3'-trifiuorometl1yl-benzophenone hydrochloride, M.P. -134".

4-(2,3-epoxy-propoxy)-4'-fluorobenzophenone and 4-pchlor0phenyl-1,2,3,6 tetrahydropyridine; the compound 4 [3- (4- (p-chlorophenyl) -3,6-dihydro-1 (2H) -pyridyl -2- hydroxypropoxy] 4-fluorobenzophenone hydrochloride, M.P. 204-206".

4-(2,3-epoxy-propoxy)-4'-bromobenzophenone and 4-pfiuorophenyl 1,2,3,6 tetrahydropyridine; the compound 4-[3 (4-(p-fluorophenyl)-3,6-dihydro-1(2H)-pyridyl)-2- hydroxypropoxy] 4-bromobenzophenone hydrochloride, M.P. 233.

4-(2,3-epoxy-propoxy)-4'-bromobenzophenone and 4- (p-chlorophenyl) 1,2,3,6 tetrahydropyridine; the compound 4 [3-(4-p-chlorophenyl)-3,6-dihydro-l (2H)-pyridyl) Z-hydroxypropoxy]-3'-bromobenzophenone hydrochloride, M.P. 217.

4 (2,3-epoxy-propoxy)-diphenyl-methane and 4-phenyl-1,2,3,G-tetrahydropyridine; the compound a[(p-benzylphenyloxy)-methyl] 2,6 dihydro-4phenyl-1(2H)-pyridine ethanol hydrochloride, M.P. 191.

The 4-[2,3-epoxy-propoxy] 3 methyl-benzophenone can, for example, be manufactured as follows:

10.6 g. of 4-hydroxy-3-methyl-benzophenone, 50 g. of epichlorohydrin and 3 drops of piperidine are heated on the steam bath for 12 hours. The reaction solution is freed from excess epichlorohydrin under reduced pressure. The above residue is dissolved in 20 ml. of chloroform and, after addition of 20 ml. of 3 N caustic soda, shaken at room temperature for 1 hour. The organic phase is separated, washed with water, dried over calcium chloride and evaporated to dryness. The residual oily crude 4-[2,3-ep0xy propoxy]-3-methyl-benzophenone crystallizes after long standing. The compound can be further processed without further purification. The compound, recrystallized from aqueous ethyl alcohol, melts at 56- 58. The 4-[2,3-epoxy propoxy]-4-methoxy-benzophenone manufactured in an analogous manner from 4-hydroxy-4-methoxy-benzophenone melts at l23-124. The ether'4-[2,3 epoxy propoxy] -benzophenones identified above can be prepared similarly.

Example 2 5.1 g. of 4-[2,3-epoxy-propoxy]benzophenone are dissolved in 20 ml. of dioxan and, after addition of 3.9 g. of l-o-methoxy-phenyl-piperazine, heated under reflux conditions for 5 hours. The solvent is subsequently evaporated off under reduced pressure. The residue is dissolved in 10 ml. of ethanol and made congo-acid with ethanolic hydrochloric acid. The 4-[3-(4-(o-rnethoxyphenyl)-piperazino)-2-hydroxy propoxy] benzophenone hydrochloride crystallizing out on trituration melts at 210-2l1 after recrystallization from ethanol.

In an analogous manner, there are obtained when employing:

4-[2,3-epoxy-propoxy]-benzophenone and 4-(p-chlorophenyl)-piperazine; the compound 4-[3-(4-(p-chlorophenyl)-l-piperazinyl)-2-hydroxy-propoxy]-benzophenone hydrochloride, M.P.

4 [2,3 epoxy-propoxy]-benzophenone and l-(p-methoxy-phenyl)-piperazine; the compound 4-[3-(4-(p-me- 15 thoxy-phenyl)-1-piperazinyl) 2 hydroxy-propoxyJ-benzophenone hydrochloride, M.P. 145.

4-(2,3-epoxy propoxy) benzophenone and l-m-methoxy-phenyl-piperazine; the compound 4-[3-(4-m-methoxy-phenyl)-1-piperazinyl) 2 hydroxy-propoxy1-benzophenone dihydrochloride, M.P. 193-196.

4-(2,3-epoxy-propoxy)-4'-chlorobenzophenone and 1-0- methoxy-phenyl-piperazine; the compound 4- [3-(4-(o-methoxy-phenyl)-1-piperazinyl) 2 hydroxy-propoxy-4'- chlorobenzophenone hydrochloride, M.P. 201.

4-(2,3-epoxy-propoxy)-4-fluorobenzophenone and l-pchlorophenyl-piperazine; the compound 4 -[3-(3-(p-chlorophenyl)-1-piperazinyl)-2-hydroxy propoxy]-4'-fluoro benzophenone dihydrochloride, M.P. 191-193.

4-[2,3-epoxy-propoxy]-benzophenone and N phenylpiperazine; the compound 4-[2-hydroxy-3-(4-phenyl-1- piperazinyl)-propoxy]-benzophenone hydrochloride, M.P. 210-21 1 4-(2,3-epoxy-propoxy)-benzophenone and 4-(o-chlorophenyl)-piperazine; the compound 4-[3-(4-(o-chlorophenyl) -1-piperazinyl) -2-hydroxy-propoxy] -benzophenone, hydrochloride, M.P. 179-180".

4-[2,3-epoxy propoxy] benzophenone and l-p-tolylpiperazine; the compound 4-[3-(4-(p-tolyl-1-piperazinyl)- 2-hydroxy-propoxy]-benzophenone, M.P. 128.

Example 3 2.25 g. 4-[3-(3,6-dihydro-4-phenyl-1(2H)-pyridyl) 2- hydroxypropoxy] benzophenone hydrochloride are dissolved in 500 ml. of 96% ethyl alcohol and, after addition of 0.3 g. of 5% palladium/carbon, hydrogenated at room temperature under normal pressure. After uptake of the theoretical amount of hydrogen, the catalyst is filtered 01f. The solution is evaporated almost to dryness under reduced pressure and treated with a little absolute ethyl ether. The 4-[3-(4-phenyl-piperidino) 2 hydroxypropoxyJbenzophenone hydrochloride which precipitates crystalline melts at 175-177 after recrystallization from ethanol.

Example 4 1.0 gram of 4-[3-(3,6-dihydro 4 phenyl-1(2H)-pyridyl)-2-hydroxypropoxy]benzophenone in ml. of abs. pyridine was reacted with 2 ml. of acetic anhydride. The reaction mixture was allowed to stand for 12 hours at room temperature. It was then added to 50 ml. of water and extracted with ether several times. The combined ether solution were evaporated leaving an oil which was dissolved in ethyl alcohol and with alcoholic hydrochloric acid made Congo acid. Upon the addition of ether, there was obtained crystalline 4-[3-(3,6-dihydro-4-phenyl 1- (2H)-pyridyl)-2-acetoxy-propoxy] -benzophenone hydrochloride which upon recrystallization from ethanol/ether was found to have a melting point of 181-182".

Example 5 In an analogous manner to that set forth in Example 4, 1-[(P-benzyl-phenyloxy)-methyl] 2 [3,6 dihydro 4- phenyl-(ZH) pyridine], ethanol was converted to 1-[(P- benzyl-phenyloxy)-methyl]-2-[3,6-dihydro 4 phenyl-l (2H)pyridyl]ethyl acetate hydrochloride of melting point 178.

Example 6 2.0 g. of 4-[3-(3,6-dihydro-4-phenyl-1(2H)pyridyl)-2- hydroxy-propoxy]-benzophen0ne was added to a mixture of 15 ml. of dimethyl sulfoxide and 10 ml. of acetic anhydried. The reaction mixture so obtained was allowed to stand for 24 hours at room temperature. It was then added to an excess of water and treated until neutral with 2 N sodium hydroxide. The oil which formed was taken out by extraction with ether. The ether of the ether extract was removed by evaporation yielding 4-[3-(3,6-dihydr0- 4-phenyl-l (2 H) pyridyl)-2-oxo propoxy] -benzophenone which upon treatment with alcoholic hydrochloric acid 16 yielded the hydrochloride thereof. Upon recrystallization from ethanol, the hydrochloride melted at 179180.

In an analogous manner, there are obtained when employing: 1-[(p-benzyl-phenoyloxy) -methyl] -2[3,6 dihydro-4-phenyl-1 (2H) pyrdine] -ethanol hydrochloride; the compound l-(p-benzyl-phenyloxy)-3-[3,6 dihydro 4- phenyl-l(2H)pyridyl]-propane 2 one hydrochloride, M.P. 176.

Example 7 4.5 g. of 4-[3-(3,6-dihydro-4-phenyl-1(2H)pyridyl)-2- hydroxy-propoxy]-benzophenone hydrochloride was dissolved in 10 g. of abs. pyridine. To the resultant medium, there was carefully added with stirring, 1.9 g. of p-toluene sulfonic acid chloride. The so-formed reaction medium was warmed for 1 hour in the steam bath, then cooled and poured over ice. A precipitate which formed was recrystallized from methanol to give 1-[(p-benzoyl-pheny1oxy)- methyl]-2-[3,6-dihydro-4-phenyl-1(2H)-pyridyl] ethylp-toluene sulfonate which melted at 198-200.

Example 8 Example 9 4-[3-(4-(o-methoxyphenyl) l piperazinyl) 2 hydroxy-propoxy]-benzophenone hydrochloride was treated in a manner described in the above example whereby to obtain 4-[3-(4-(0 methoxyphenyl) 1 piperazinyl)-2- hydroxy-propoxy]-benzhydrol hydrochloride of melting point 173.

Example 10 8.26 g. of 4-[3-(3,6-dihydro-4-phenyl-l(2H)Pyridyl)- Z-hydroxy-propoxy]-benzophenone and 1.53 grams of hydroxylamine hydrocholride in 4 ml. of abs. pyridine and 200 ml. of abs. ethanol were heated at for 15 hours in an autoclave. After removing the ethanol under reduced pressure, the oil which remained was added with 200 ml. of acetic ether and 100 ml. of soda lye. Crystalline 4-[3-(3,6-dihydro-4-phenyl-1(2H)-Pyrid l) 2 hydroxy-propoxy]-benzophenone oxime precipitated which upon recrystallization from methanol was found to have a melting point of 178.

Example 11 4-[3-(3,6-dihydro-4-phenyl 1(2H)pyridy1)-2-hydroxypropoxy]-4'-chloro-benzophenone was treated with hydroxylamine hydrochloride in the manner set out in the preceding example thereby to obtain 4-[3-(3,6-dihydro-4- phenyl-l(2H)-pyridyl)-2-hydroxy-propoxy] 4' chlorobenzophenone oxime of melting point 178182.

Example 12 To a mixture of 25 g. of o-phosphoric acid and 5 g. of phosphoric pentoxide, there was carefully added with stirring at 60 over a period of 1 hour, 4.5 g. of 4-[3- (3,6-dihydro-4-phenyl-1(2H)pyridyl) 2 hydroxy-propoxyj-benzophenone hydrochloride. The reaction mixture was stirred for an additional 4 hours at 60. The hydrogen chloride which formed was removed from time to time by evaporation. After cooling and diluting with water, the oil which formed was cooked for 20 minutes with 30 ml. of 2 N hydrochloric acid. Upon cooling, crystalline 1[(p-benzoyl-phenoxy)-1nethyl]-2-[3,6-dihydro 4 phen- 1 7 yl 1(2H)pyridyl] ethyl-orthophosphate was obtained which melted at 246-248.

Example 13 4.48 grams of 4-[3%3,6-dihydro-4-phenyl-1(2H)pyridyl)-2-hydroxy-propoxy] -4-chlorobenzophenone and 1.06 grams of sodium carbonate were suspended in 50 ml. of acetone with stirring and treated under refluxing conditions with a solution of 1.89 grams of the methyl ester of chloroformic acid in 10 ml. of acetone. The resulting reaction mixture was refluxed for an additional 6 hours and then left to stand over a period of 12 hours at room temperature. The precipitated sodium chloride was removed by filtration. The solution was evaporated to dryness under reduced pressure. The residue was added to benzene and adsorbed on silica gel (kieselgel). Upon extraction from the gel, there was obtained 1-[(Parachlorobenzoylphenoxy) methyl] 2 [3,6 dihydro-4- phenyl-l(2H)pyridyl]-ethyl methyl carbonate which after recrystallization from methanol is found to melt at 9396.

Example 14 4.5 g. of 4-[3-(3,6-dihydro-4-phenyl-1(2H)pyridyl)-2- hydroxy-propoxy]-benzophenone was suspended in 400 ml. of benzene and treated under refluxing conditions. A stream of gaseous hydrochloric acid was conducted through the suspension for one hour. Afterwards 6.2 g. of distilled ethylene glycol and 3.44 g. of p-toluene sulphonic acid were added. The resulting clear solution was evaporated under reduced pressure. The residue was dissolved in acetic ether. The solution was washed three times with 1 N sodium hydroxide, dried over sodium sulfate and evaporated under reduced pressure. The 3,6-dihydro 4 phenyl a [(p-(Z-phenyl-1,3-dioxolane-2-yl)- phenyloxy) methyl] l(2H)-pyridine ethanol melted at 120 C. after recrystallization from methanol.

In an analogous manner there were obtained when employing: 4-[3-(3,6 dihydro 4 phenyl-1(2H)-pyridyl)- 2-hydroxypropoxy]-benzophenone and 1,3 propanediol; the compound 3,6 dihydro-4-phenyl-a-[(p-(2-phenyl-mdioxane 2-yl)-phenyloxy)methyl] 1(2H) pyridine ethanol, M.P.: 116.5" C.

Example 15 4.74 g. of 4-hydroxy-benzophenone were added to a solution of 552 mg. sodium in 100 ml. ethanol. The mixture was heated under refluxing conditions and treated dropwise with a solution of 6 g. 1-[4-phenyl-1,2,3,6-tetrahydro-pyridyl] 2 hydroxy-3-chloro-propane in 100 ml. abs. ethanol. The reaction mixture was heated to boiling for 4 hours, then evaporated under reduced pressure. The oily residue was dissolved in acetic ether. The solution was washed twice with 1 N sodium hydroxide, with water, dried over sodium sulfate and evaporated under reduced pressure. The 4 [3-(3,6-dihydro-4-phenyl-l (2H)pyridyl) 2 hydroxy propoxy]-benzophenone was recrystallized twice from isopropanol. The hydrochloride of this compound melted at 192194.

The starting material 1 [4-phenyl-l,2,3,6-tetrahydropyridyl]-2-hydroxy-3-chloro-propane was prepared as follows: 6.37 g. of 4-phenyl-1,2,3,6-tetrahydro-pyridine, 2 drops of piperidine and 40 ml. of abs. ethyl ether were cooled to and for a period of 30 minutes treated with 3.70 g. of epichlorohydrine in ml. of abs. ethyl ether. The reaction mixture was allowed to stand for 24 hours at room tempearture and then left to stand for a period of 60 hours at about 0. Then the solution was filtered and evaporated under reduced pressure. The oily residue was dissolved in benzene, adsorbed on silica gel [kieselgel] [granulation 0.20.5 mm] and extracted with benzene/ethyl-ether 4:1. After evaporation under reduced pressure, the oily residue was treated with charcoal, filtered and evaporated under reduced pressure. The crystalline 1-[4-phenyl-1,2,3,6-tetrahydro-pyridyl]-2-hydroxy-3- chloro-propane melted at 695-71".

18 Example 16 3.55 g. of 1-[4-phenyl-1,2,3,6-tetrahydro-pyridyl]-2,3- epoxy-propane, 3.37 g. of 4-hydroxy-benzophenone, 2

drops of piperidine were, after addition of 50 ml. di-

oxane, boiled under reflux for 15 hours. Then the reaction mixture was evaporated under reduced pressure. The oily residue was dissolved in acetic ether. The solution was washed twice with 1 N sodium hydroxide, with water, dried over sodium sulfate and evaporated under reduced pressure. The residue was dissolved in benzene. The solution was adsorbed on silica gel. After evaporation of the extract the oily 4-[3-(3,6-dihydro-4-phenyl- 1(2H)pyridyl) 2 hydroxy-propoxy] -benzophenone was recrystallized twice from isopropanol. The hydrochloride of this compound melted at 192-194".

The starting material 1-[4-phenyl-1,2,3,6-tetrahydropyridyl]-2,3-epoxy-propane was prepared as follows: 6.37 g. of 4-phenyl-1,2,3,6-tetrahydro-pyridine were, after the addition of 2 drops of piperidine, treated dropwise under stirring and cooling with 3.7 g. of epicholorohydrine. The reaction mixture was allowed to stand for 12 hours at room temperature and then left to stand for a period of 60 hours at about 0. Then the oil was dissolved in chloroform. The solution of 30 ml. of 3 N sodium hydroxide was added and shook for 1 hour. After separation of the aqueous layer the chloroform extract was washed with water, dried over sodium sulfate and evaporated under reduced pressure. The oily residue was dissolved in benzene, adsorbed on silica gel [kieselgel] and extracted with benzene/ethyl ether 4:1. After evaporation the remaining oily 1-[4-phenyl-1,2,3,6-tetrahydropyridyl]-2,3-epoxy-propane can be further processed without further purification.

Example 17 27.2 g. of 4-(2,3-epoxypropoxy)-4'-fluorobenzophenone and 19.2 g. 1-(p-methoxyphenyl)piperazine are refluxed for 1 hour with 500 ml. ethanol. After cooling, the separated crystals are filtered and washed with a small volume of ether. 4-{3-[4-(p-methoxyphenyl)-1-piperazinyl]-2-hydroxypropoxy}-4'-fluorobenzophenone is obtained; it melts at 149-150 C. after crystallization from acetonitrile.

The starting material 4-(2,3-epoxypropoxy)-4'-fluorobenzophenone can be prepared in the following manner.

23 g. of 4-methoxy-4'-fluorobenzophenone are added with agitation to a hot mixture of 3 0 ml. glacial acetic acid and 60 ml. 65 percent hydrobromic acid and refluxed with continued agitation. The hot solution is poured into approximate 200 ml. water; a precipitate is formed. The mixture is filtered after cooling. The residue is washed neutral with water and dissolved in an excess of warm 3 N soda lye. The solution is extracted with chloroform. The aqueous phase is acidified with concentrated hydrochloric acid. The separate crude product is filtered, washed neutral with water and crystallized from a mixture of water and ethanol (1:3). The 4-hydroxy-4'-fluorobenzophenone is obtained in crystals that melt at 170 172 C.

21.6 g. of 4-hydroxy-4'-fluorobenzophenone, 40 ml. epichlorohydrin and 0.3 ml. piperidine are stirred for 12 hours at C. The excess epichlorohydrin is evaporated under reduced pressure at 80 C. The residue is dissolved in approximately 50 ml. chloroform and shaken for 1 hour with a solution of 4 g. sodium hydroxide in 10 ml. water. The aqueous phase is separated, the organic phase is washed neutral with water, dried over potassium carbonate and evaporated. 4-(2,3-epoxypropoxy)-4'-fluorobenzophenone crystals are obtained after crystallization from methanol; they melt at -106 C.

Example 18 Rac. 4-{3-[4-(p methoxyphenyl)-l-piperizinyl]-2-hydroxypropoxy}-4-chlorobenzophen0ne is obtained in the manner described in Example 17 from 4-(2,3-epoxyp1'o- 19 poxy)-4'-chlorobenzophenone and l-(p-methoxyphenyD- piperazine. It melts at 150-151 C. after recrystallization from ethanol.

The starting material 4(2,3-epoxypropoxy)-4'-chlorobenzophenone can be prepared in a manner similar to that of Example 14. The melting point is 116-1l7 C. (from ethanol).

Example 19 1 g. of 4-hydroxy-4'-fluorobenzophenone is added to a solution of 120 mg. sodium in 20 ml. absolute ethanol. A solution of 1.4 g. rac. 1-(2-hydroxy-3-chloropropyl)-4- (p-methoxyphenyl) piperazine in ml. absolute ethanol is added to the above solution. The obtained mixture is refluxed for 1.5 hours. Rac. 4-{3-[4-(p-methoxyphenyl)- l-piperazinyl] 2 hydroxypropoxy} 4' fluorobenzophenone is obtained in crystalline form after cooling. The crystals obtained by crystallization from acetonitrile melt at 149'-150 C.

The starting material rac. l-(2-hydroxy-3-chloropropyl)-4-(p-methoxyphenyl)piperazine can be prepared as follows: 3.8 g. of l-(p-methoxyphenyl)piperazine are dissolved in ml. methanol and reacted with 2 g. epichlorohydrin. The reaction mixture is allowed to stand for 24 hours at room temperature; the crude product separates out in crystalline form during this period. Pure rac. 1-(2- hydroxy 3 chloropropyl) 4 p-methoxyphenyl)piperazine is obtained after filtering and crystallization from ethanol; it melts at 111 to 111.5 C.

Example 20 Using 4-hydroxy-4'-chlorobenzophenone and rac. 1-(2- hydroxy-3-chloropropyl)-4-(para methoxyphenyl)piperazine in the manner described in Example 19, rac. 4-{3- [4 (p-methoxyphenyl)-1-piperazinyl] 2 hydroxypropoxy}-4'-chlorobenzophenone is obtained; it melts at 150- 151 C. after crystallization from ethanol.

Example 21 0.5 g. of rac. 4-{3-[(2-p-anisidinoethyl)amino]-2-hydroxypropoxy}-4'-fluorobenzophenone and 0.2 g. 1,2 dibromoethane are heated for 24 hours on the steam bath. After cooling, the reaction mixture is mixed with ether and freed from insoluble components by filtration. After evaporation of the ether, the residue is mixed with chloroform and 3 N ammonia solution. The organic phase is dried over potash and the solvent is evaporated under reduced pressure. The residue is chromatographed on silica gel with absolute ether as the solvent. The obtained pure rac. 4 ({3-[4-(p-methoxyphenyl)-1 piperazinyl] 2 hydroxypropoxy}4'-fluorobenzophenone melts at 142 C.

The starting material rac. 4-{3-[(2-p-anisidinoethyl)- amino]-2-hydroxypropoxy}-4-fluorobenzophenone can be prepared as follows: 8.1 g. of 4-(2,3 epoxypropoxy)-4- fluorobenzophenone and g. ethyleneimine are allowed to stand for 24 hours at room temperature in 200 ml. methanol. The excess ethyleneimine and the solvent are evaporated under reduced pressure and the residue is crys tallized from ethylacetate and petroleum ether. The obtained rac. 4-[3-(l-aziridinyl) 2 hydroxypropoxy]-4'- fluorobenzophenone melts after a second crystallization at 117-118 C.

2.6 g. of rac. 4-[3-(l-aziridinyl)-2-hydroxypropoxy]- 4' fluorobenzophenone, 1.1 g. p-anisidine and 2.5 g. maleic acid are allowed to stand in 18 ml. methanol for 4 days at room temperature; crude rac. 4-{3-[(2-anisidinoethyl)amino] 2 hydroxypropoxy} 4 fluorobenzophenone maleinate crystallizes out. The crystallization is completed by keeping in the refrigerator. After crystallization from ethanol, the product melts at 165167 C.

Example 22 1.6 g. of rac. 4-(3-amino-2-hydroxypropoxy)-4-fluorobenzophenone HCl, 1.7 g. bis-N,N-(2 bromoethyD-panisidine and 0.6 g. sodium hydroxide are refluxed for 20 24 hours in 30 ml. n-butanol and filtered while hot. The rac. 4-{3-[4-(p-methoxyphenyl) 1 piperazinyl]-Z-hydroxypropoxy} 4' fluorobezophenone, crystallizing on cooling and after rubbing, melts at 147 C. after crystallization from methanol.

The starting material rac. 4-(3 amino-2-hydroxypropoxy) 4' fluorobenzophenone HCl can be prepared as follows: 2.7 g. of 4-(2,3-epoxypropoxy)-4'-fluorobenzophenone and 1.0 g. succinimide are refluxed for 5 hours in 20 ml. ethanol. The N-{3-[p-(p-fluorobenzoyl)-phenoxy]-2-hydroxypropyl}succinimide crystallizing on cooling melts at 155-l57 C. after recrystallization from ethanol.

13.6 g. of N {3 [p (p fluorobenzoyl) phenoxyl]- 2 hydroxy-propyl}succinimide are refluxed with ml. concentrated hydrochloric acid for 16 hours. After evapoation of the excess hydrochloric acid under reduced pressure, the residue is made alkaline with l N soda lye. The crude base is filtered, dissolved in methanol and converted to the corresponding hydrochloride by the addition of methanolic hydrochloric acid. The rac. 4-(3-amino-2-hydroxypropoxy)-4-fluorobenzophen0ne HCl obtained in this manner melts at 250251 C. after crystallization from methanol.

Example 23 0.5 g. of rac. 4 {3 [4 (p hydroxyphenyl) 1- piperazinyl] 2 hydroxypropoxy} 4' fluorobenzophenone are dissolved in 100 ml. methanol and mixed with excess solution of diazomethane in ether. The solution is allowed to stand at room temperature for 12 hours and is evaporated under reduced pressure until crystallization begins. The obtained rac. 4 {3 [4 (p methoxyphenyl) 1 piperazinyl] 2 hydroxypropoxy} 4'- fluorobenzophenone melts, after crystallization from methanol, at 144-146 C.

The starting material rac. 4 {3 [4 (p hydroxyphenyl) 1 piperazinyl] 2 hydroxypropoxy} 4'- fluorobenzophenone can be prepared as follows: 5.5 g. of 4 (2,3 epoxypropoxy) 4' fluorobenzophenone and 3.6 g. 1-(p-hydroxyphenyl)piperazine are refluxed for 1 hour in 40 ml. ethanol. The solvent is evaporated under reduced pressure, the oily residue is acidified with ethanolic hydrochloric acid and crystallized with ethylacetate. The obtained rac. 4 {3 [4 (p hydroxyphenyl) lpiperazinyl] 2 hydroxypropoxy} 4' fluorobenzophenone melts, after recrystallization from water at 184-186 C.

Example 24 Example 25 Capsule dosage forms containing the following contents:

s 4 [3 (3,6 dihydro 4 phenyl 1(2H) pyridyl)- 2 hydroxy propoxy] benzophenone hydrochloride l0 Mannitol Talcum 5 were prepared as follows:

4 [3 (3,6 dihydro 4 phenyl 1(2H) pyridyl)- 2 hydroxy propoxy] benzophenone hydrochloride is 21 homogeneously mixed with the talcum and mannitol, passed through a No. sieve (mesh width about 0.23 mm.) and again thoroughly mixed. The mixture obtained is filled into gelatin capsules No. 4.

Example 26 Dragee dosage forms containing the following ingredients:

Mg. 4 [3 (4 (o methoxy phenyl) piperazino) 2- hydroxy-propoxy]-benzophenone hydrochloride..- 25 Mannitol 100 Maize starch 20 Talcum 5 were manufactured as follows:

22 We claim: 1. A compound of the formula MQEQZLQQM wherein R is hydrogen or halogen and R is hydrogen, halogen or lower alkoxy the pharmaceutically acceptable acid addition salts thereof, the quaternary salts thereof with quaternizing agents, the ketals thereof formed by reaction of the benzophcnone compound with a lower alkanol or ethylene glycol and optical isomers thereof.

2. The compound of claim 1 wherein R and R are hydrogen i.e. 4-[3-(4-phenyl-piperidino)-2-hydroxy-propoxy] benzophenone.

References Cited UNITED STATES PATENTS 3,674,799 7/1972 Edenhofer et al. 260--293.8

JOHN D. RANDOLPH, Primary Examiner S. D. WINTERS, Assistant Examiner US. Cl. X.R. 260-29357, 293.83

UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,816,434 DATED :June ll, 1974 lNV ENTOR(S) Albrecht Edenhofer, Henri Ramuz and Hans Spiegelberg It is certified that error appears in the ab0veidentified patent and that said Letters Patent are hereby corrected as shown below: 1

Column 1, line 12 after "245,609" insert Foreign Application Priority Data Q July 30, 1965 Switzerland 107-69/65 Claim 2,' lines 14-17 which reads 0 "of, the quaternary salts thereof with quaternizing I agents, the ketals thereof formed by reaction of the benzophenone compound with a lower alkanol or ethy- U lene glycol and optical isomers thereof."

should be of, formed by reaction of the benzophenone compound with a lower alkanol or ethylene glycol, the

quaternary salts thereof with quaternizing agents,

the ketals thereof and optical isomers thereof. i

Signed and Scaled this a [SEAL] Sixth Day of July 1976 Arrest:

0 :Sl'l ig ig" c. MARSHALL DANN ummissioner oflarems and Trademarks 

